A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034874



Internal ID18777406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76977978..77212740hg38UCSC Ensembl
Innerchr7:76607295..76842057hg19UCSC Ensembl
Innerchr7:76445231..76679993hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38234763
hg19234763
hg18234763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657114
Samples
Known GenesCCDC146, DTX2P1-UPK3BP1-PMS2P11, FGL2, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034874
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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